The Regulation and Secretion of Glucagon in Response to Nutrient Composition: Unraveling Their Intricate Mechanisms
- PMID: 37764697
- PMCID: PMC10536047
- DOI: 10.3390/nu15183913
The Regulation and Secretion of Glucagon in Response to Nutrient Composition: Unraveling Their Intricate Mechanisms
Abstract
Glucagon was initially regarded as a hyperglycemic substance; however, recent research has revealed its broader role in metabolism, encompassing effects on glucose, amino acids (AAs), and lipid metabolism. Notably, the interplay of glucagon with nutrient intake, particularly of AAs, and non-nutrient components is central to its secretion. Fasting and postprandial hyperglucagonemia have long been linked to the development and progression of type 2 diabetes (T2DM). However, recent studies have brought to light the positive impact of glucagon agonists on lipid metabolism and energy homeostasis. This review explores the multifaceted actions of glucagon, focusing on its regulation, signaling pathways, and effects on glucose, AAs, and lipid metabolism. The interplay between glucagon and other hormones, including insulin and incretins, is examined to provide a mechanistic understanding of its functions. Notably, the liver-α-cell axis, which involves glucagon and amino acids, emerges as a critical aspect of metabolic regulation. The dysregulation of glucagon secretion and its impact on conditions such as T2DM are discussed. The review highlights the potential therapeutic applications of targeting the glucagon pathway in the treatment of metabolic disorders.
Keywords: amino acid; glucagon; glucose; hyperglucagonemia; lipid.
Conflict of interest statement
The authors declare no conflict of interest.
Figures
![Figure 1](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f58/10536047/b374166ba17d/nutrients-15-03913-g001.gif)
![Figure 2](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f58/10536047/2f897a6706d4/nutrients-15-03913-g002.gif)
Similar articles
-
Inhibition of glucagon secretion.Adv Pharmacol. 2005;52:151-71. doi: 10.1016/S1054-3589(05)52008-8. Adv Pharmacol. 2005. PMID: 16492545 Review.
-
The role of alpha-cell dysregulation in fasting and postprandial hyperglycemia in type 2 diabetes and therapeutic implications.Endocr Rev. 2007 May;28(3):253-83. doi: 10.1210/er.2006-0026. Epub 2007 Apr 4. Endocr Rev. 2007. PMID: 17409288 Review.
-
Hyperglucagonemia correlates with plasma levels of non-branched-chain amino acids in patients with liver disease independent of type 2 diabetes.Am J Physiol Gastrointest Liver Physiol. 2018 Jan 1;314(1):G91-G96. doi: 10.1152/ajpgi.00216.2017. Epub 2017 Sep 28. Am J Physiol Gastrointest Liver Physiol. 2018. PMID: 28971838
-
The Liver-α-Cell Axis in Health and in Disease.Diabetes. 2022 Sep 1;71(9):1852-1861. doi: 10.2337/dbi22-0004. Diabetes. 2022. PMID: 35657688 Free PMC article. Review.
-
Enteroinsular signaling: perspectives on the role of the gastrointestinal hormones glucagon-like peptide 1 and glucose-dependent insulinotropic polypeptide in normal and abnormal glucose metabolism.Curr Opin Clin Nutr Metab Care. 2003 Jul;6(4):461-8. doi: 10.1097/01.mco.0000078991.96795.84. Curr Opin Clin Nutr Metab Care. 2003. PMID: 12806222 Review.
Cited by
-
The role of mu-opioid receptors in pancreatic islet alpha cells.bioRxiv [Preprint]. 2024 May 15:2024.05.13.593899. doi: 10.1101/2024.05.13.593899. bioRxiv. 2024. Update in: J Mol Endocrinol. 2024 Dec 20;74(1):e240060. doi: 10.1530/JME-24-0060. PMID: 38798528 Free PMC article. Updated. Preprint.
References
-
- Ricketts H.T. Glucagon: Molecular Physiology, Clinical and Therapeutic Implications. JAMA. 1973;224:403. doi: 10.1001/jama.1973.03220160053031. - DOI
-
- Murlin J.R., Clough H.D., Gibbs C.B.F., Stokes A.M. Aqueous Extracts of Pancreas. J. Biol. Chem. 1923;56:253–296. doi: 10.1016/S0021-9258(18)85619-8. - DOI
-
- Guzman C.B., Zhang X.M., Liu R., Regev A., Shankar S., Garhyan P., Pillai S.G., Kazda C., Chalasani N., Hardy T.A. Treatment with LY2409021, a glucagon receptor antagonist, increases liver fat in patients with type 2 diabetes. Diabetes Obes. Metab. 2017;19:1521–1528. doi: 10.1111/dom.12958. - DOI - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical